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1.
PLoS One ; 11(1): e0146932, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26752173

RESUMO

Immaturity of the neonatal immune system is causative for high morbidity in calves and colostrum intake is crucial for acquiring passive immunity. Pathogenesis is promoted by reactive oxygen species accumulating at birth if counter-regulation is inadequate. The flavonol quercetin exerts antioxidative and anti-inflammatory effects that may enhance neonatal health. The aim of this work was to study effects of quercetin feeding on metabolic, antioxidative and inflammatory parameters in neonatal calves to investigate whether quercetin could compensate for insufficient colostrum supply. Twenty-eight newborn calves were assigned to two dietary groups fed colostrum or milk-based formula on day 1 and 2 and milk replacer thereafter. From day 2 onwards, 7 calves per diet group were additionally fed quercetin aglycone (50 mg/(kg body weight × day)). Blood samples were taken repeatedly to measure plasma concentrations of flavonols, glucose, lactate, total protein, albumin, urea, non-esterified fatty acids, triglycerides, cholesterol, insulin, glucagon, cortisol, immunoglobulins, fibrinogen, haptoglobin and serum amyloid A. Trolox equivalent antioxidative capacity, ferric reducing ability of plasma, thiobarbituric acid reactive species and F2-isoprostanes were analyzed to evaluate plasma antioxidative status. Expression of tumor necrosis factor, interleukin-1α, interleukin-1ß, serum amyloid A, haptoglobin, fibrinogen, C-reactive protein, catalase, glutathione peroxidase and superoxide dismutase mRNA were measured in liver tissue on day 8. Plasma flavonol concentrations were detectable only after quercetin-feeding without differences between colostrum and formula feeding. Plasma glucose, lactate, total protein, immunoglobulins, triglycerides, cholesterol, trolox equivalent antioxidative capacity and thiobarbituric acid reactive species were higher after colostrum feeding. Body temperature, fecal fluidity and plasma concentrations of cortisol and haptoglobin were higher in formula- than in colostrum-fed groups. Hepatic mRNA expression of tumor necrosis factor was higher after quercetin feeding and expression of C-reactive protein was higher after formula feeding. Data confirm that colostrum improves neonatal health and indicate that quercetin feeding cannot compensate for insufficient colostrum supply.


Assuntos
Fenômenos Fisiológicos da Nutrição Animal , Antioxidantes/química , Colostro/química , Inflamação/metabolismo , Leite/química , Quercetina/uso terapêutico , Administração Oral , Ração Animal , Animais , Animais Recém-Nascidos , Glicemia/análise , Temperatura Corporal , Proteína C-Reativa/metabolismo , Bovinos , Colesterol/sangue , Cromanos/sangue , Cromanos/química , F2-Isoprostanos/metabolismo , Fezes , Feminino , Flavonóis/sangue , Haptoglobinas/metabolismo , Hidrocortisona/metabolismo , Imunoglobulinas/sangue , Ácido Láctico/sangue , Fígado/metabolismo , Substâncias Reativas com Ácido Tiobarbitúrico , Triglicerídeos/sangue , Fator de Necrose Tumoral alfa/metabolismo
2.
J Nutr ; 145(11): 2486-95, 2015 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-26400967

RESUMO

BACKGROUND: Inadequate colostrum supply results in insufficient intake of macronutrients and bioactive factors, thereby impairing gastrointestinal development and the maturation of glucose metabolism in neonatal calves. The flavonoid quercetin has been shown to have health-promoting properties, including effects in diabetic animals. However, quercetin interacts with intestinal glucose absorption and might therefore exert negative effects in neonates. OBJECTIVE: We evaluated the interaction between neonatal diet and quercetin feeding on splanchnic glucose metabolism in neonatal calves. METHODS: Calves (n = 28) were assigned to 4 groups and fed either colostrum or a milk-based formula on days 1 and 2 and supplemented daily with 148 µmol quercetin aglycone/kg body weight [colostrum with quercetin (CQ+)/formula with quercetin (FQ+)] or without this substance [colostrum without quercetin (CQ-)/formula with quercetin (FQ-)] from days 2-8. From day 3 onward, all calves received milk replacer. A xylose absorption test was performed on day 3, and on day 7, blood samples were collected to study glucose first-pass uptake after [(13)C6]-glucose feeding and intravenous [6,6-(2)H2]-glucose bolus injection. Plasma concentrations of metabolites and hormones were measured by taking additional blood samples. A biopsy specimen of the liver was harvested on day 8 to measure the mRNA expression of gluconeogenic enzymes. RESULTS: Higher postprandial plasma concentrations of glucose, lactate, urea, adrenaline, noradrenaline, insulin, and glucagon on day 7 in colostrum-fed calves indicate that metabolic processes were stimulated. Postabsorptive xylose and glucose plasma concentrations each increased by an additional 26%, and splanchnic glucose turnover decreased by 35% in colostrum-fed calves, suggesting improved glucose absorption and lower splanchnic glucose utilization in colostrum-fed calves. Quercetin supplementation resulted in higher noradrenaline concentrations and enhanced peak absorption and oxidation of [(13)C6]-glucose by 10%. Liver mitochondrial phosphoenolpyruvate carboxykinase mRNA abundance was reduced by 34% in colostrum-deprived calves. CONCLUSIONS: Feeding colostrum during the first 2 d of life is crucial for maturation of splanchnic glucose metabolism in calves. Supplementing quercetin improves gastrointestinal absorption capacity, particularly in colostrum-deprived calves.


Assuntos
Dieta/veterinária , Glucose/metabolismo , Quercetina/administração & dosagem , Administração Oral , Fenômenos Fisiológicos da Nutrição Animal , Animais , Animais Recém-Nascidos , Glicemia/metabolismo , Bovinos , Colostro , Epinefrina/sangue , Flavonóis/sangue , Glucagon/sangue , Insulina/sangue , Absorção Intestinal , Ácido Láctico/sangue , Fígado/efeitos dos fármacos , Fígado/metabolismo , Masculino , Norepinefrina/sangue , Período Pós-Prandial , Quercetina/farmacocinética , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Ureia/sangue , Xilose/sangue
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